Mutations in the Genes Encoding the Transcription Factors Hepatocyte Nuclear Factor 1 Alpha and 4 Alpha in Maturity-Onset Diabetes of the Young and Hyperinsulinemic Hypoglycemia von Colclough, Kevin, Bellanne-Chantelot, Christine, Saint-Martin, Cecile, Flanagan, Sarah E., Ellard, Sian

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Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia von Osbak, Kara K, Colclough, Kevin, Saint-Martin, Cecile, Beer, Nicola L, Bellanné-Chantelot, Christine, Ellard, Sian, Gloyn, Anna L

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Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis von Donath, Xavier, Saint-Martin, Cécile, Dubois-Laforgue, Danièle, Rajasingham, Ramanan, Mifsud, François, Ciangura, Cécile, Timsit, José, Bellanné-Chantelot, Christine

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Pregnancy in Women With Monogenic Diabetes due to Pathogenic Variants of the Glucokinase Gene: Lessons and Challenges von Timsit, José, Ciangura, Cécile, Dubois-Laforgue, Danièle, Saint-Martin, Cécile, Bellanne-Chantelot, Christine

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Biological behaviors of mutant proinsulin contribute to the phenotypic spectrum of diabetes associated with insulin gene mutations von Wang, Heting, Saint-Martin, Cécile, Xu, Jialu, Ding, Li, Wang, Ruodan, Feng, Wenli, Liu, Ming, Shu, Hua, Fan, Zhenqian, Haataja, Leena, Arvan, Peter, Bellanné-Chantelot, Christine, Cui, Jingqiu, Huang, Yumeng

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Application of phage display to high throughput antibody generation and characterization von Schofield, Darren J, Pope, Anthony R, Clementel, Veronica, Buckell, Jenny, Chapple, Susan Dj, Clarke, Kay F, Conquer, Jennie S, Crofts, Anna M, Crowther, Sandra R E, Dyson, Michael R, Flack, Gillian, Griffin, Gareth J, Hooks, Yvette, Howat, William J, Kolb-Kokocinski, Anja, Kunze, Susan, Martin, Cecile D, Maslen, Gareth L, Mitchell, Joanne N, O'Sullivan, Maureen, Perera, Rajika L, Roake, Wendy, Shadbolt, S Paul, Vincent, Karen J, Warford, Anthony, Wilson, Wendy E, Xie, Jane, Young, Joyce L, McCafferty, John

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mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success von Szymanowski, Marie, Estebanez, Maria Salomon, Padidela, Raja, Han, Bing, Mosinska, Karolina, Stevens, Adam, Damaj, Lena, Pihan-Le Bars, Florence, Lascouts, Emilie, Reynaud, Rachel, Ferreira, Catherine, Bansept, Claire, de Lonlay, Pascale, Saint-Martin, Cécile, Dunne, Mark J, Banerjee, Indraneel, Arnoux, Jean-Baptiste

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Case report: Exceptional transmission of congenital hyperinsulinism from a focal CHI mother to her diffuse CHI dichorionic diamniotic twins von Telehuz, Daniela, Plesa, Oana, Bouilloud, Florence, Wucher, Helene, De Lonlay, Pascale, Bérat, Claire-Marine, Saint-Martin, Cécile, Dupuy, Olivier, Arnoux, Jean-Baptiste

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The Common HNF1A Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY von Locke, Jonathan M, Saint-Martin, Cécile, Laver, Thomas W, Patel, Kashyap A, Wood, Andrew R, Sharp, Seth A, Ellard, Sian, Bellanné-Chantelot, Christine, Hattersley, Andrew T, Harries, Lorna W, Weedon, Michael N

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Gene Panel Sequencing of Patients With Monogenic Diabetes Brings to Light Genes Typically Associated With Syndromic Presentations von Saint-Martin, Cécile, Bouvet, Delphine, Bastide, Mathilda, Bellanné-Chantelot, Christine

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Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B ( HNF1B ) Molecular Defects von Dubois-Laforgue, Danièle, Cornu, Erika, Saint-Martin, Cécile, Coste, Joël, Bellanné-Chantelot, Christine, Timsit, José

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Accumulation of amyloid precursor protein C-terminal fragments triggers mitochondrial structure, function, and mitophagy defects in Alzheimer’s disease models and human brains von Vaillant-Beuchot, Loan, Mary, Arnaud, Pardossi-Piquard, Raphaëlle, Bourgeois, Alexandre, Lauritzen, Inger, Eysert, Fanny, Kinoshita, Paula Fernanda, Cazareth, Julie, Badot, Céline, Fragaki, Konstantina, Bussiere, Renaud, Martin, Cécile, Mary, Rosanna, Bauer, Charlotte, Pagnotta, Sophie, Paquis-Flucklinger, Véronique, Buée-Scherrer, Valérie, Buée, Luc, Lacas-Gervais, Sandra, Checler, Frédéric, Chami, Mounia

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Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome von Depienne, Christel, Trouillard, Oriane, Gourfinkel-An, Isabelle, Saint-Martin, Cécile, Bouteiller, Delphine, Graber, Denis, Barthez-Carpentier, Marie-Anne, Gautier, Agnès, Villeneuve, Nathalie, Dravet, Charlotte, Livet, Marie-Odile, Rivier-Ringenbach, Clothilde, Adam, Claude, Dupont, Sophie, Baulac, Stéphanie, Héron, Delphine, Nabbout, Rima, LeGuern, Eric

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School level of children carrying a HNF1B variant or a deletion von Laliève, Fanny, Decramer, Stéphane, Heidet, Laurence, Baudouin, Véronique, Lahoche, Annie, Llanas, Brigitte, Cochat, Pierre, Tenenbaum, Julie, Lavocat, Marie-Pierre, Eckart, Philippe, Broux, Françoise, Roussey, Gwenaelle, Cloarec, Sylvie, Vrillon, Isabelle, Dunand, Olivier, Bessenay, Lucie, Tsimaratos, Michel, Nobili, François, Pietrement, Christine, De Parscau, Loïc, Bonneville, Valérie, Rodier, Nicolas, Saint-Martin, Cécile, Chassaing, Nicolas, Michel-Calemard, Laurence, Moriniere, Vincent, Bellanné-Chantelot, Christine, Bahans, Claire, Guigonis, Vincent

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A simple vector system to improve performance and utilisation of recombinant antibodies von Martin, Cecile D, Rojas, Gertrudis, Mitchell, Joanne N, Vincent, Karen J, Wu, Jiahua, McCafferty, John, Schofield, Darren J

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Update of variants identified in the pancreatic β-cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes von De Franco, Elisa, Saint-Martin, Cécile, Brusgaard, Klaus, Knight Johnson, Amy E, Aguilar-Bryan, Lydia, Bowman, Pamela, Arnoux, Jean-Baptiste, Larsen, Annette Rønholt, Sanyoura, May, Greeley, Siri Atma W, Calzada-León, Raúl, Harman, Bradley, Houghton, Jayne A L, Nishimura-Meguro, Elisa, Laver, Thomas W, Ellard, Sian, Del Gaudio, Daniela, Christesen, Henrik Thybo, Bellanné-Chantelot, Christine, Flanagan, Sarah E

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Detection of Partial-Body Exposure to Ionizing Radiation by the Automatic Detection of Dicentrics von Vaurijoux, Aurelie, Gregoire, Eric, Roch-Lefevre, Sandrine, Voisin, Pascale, Martin, Cecile, Voisin, Philippe, Roy, Laurence, Gruel, Gaetan

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Successful treatment of congenital hyperinsulinism with long-acting release octreotide von Le Quan Sang, Kim-Hanh, Arnoux, Jean-Baptiste, Mamoune, Asmaa, Saint-Martin, Cécile, Bellanné-Chantelot, Christine, Valayannopoulos, Vassili, Brassier, Anais, Kayirangwa, Honorine, Barbier, Valérie, Broissand, Christine, Fabreguettes, Jean-Roch, Charron, Brigitte, Thalabard, Jean-Christophe, de Lonlay, Pascale

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Inhibition of enteric methanogenesis in dairy cows induces changes in plasma metabolome highlighting metabolic shifts and potential markers of emission von Yanibada, Bénédict, Hohenester, Ulli, Pétéra, Mélanie, Canlet, Cécile, Durand, Stéphanie, Jourdan, Fabien, Boccard, Julien, Martin, Cécile, Eugène, Maguy, Morgavi, Diego P., Boudra, Hamid

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Prediction of enteric methane production, yield, and intensity in dairy cattle using an intercontinental database von Niu, Mutian, Kebreab, Ermias, Hristov, Alexander N., Oh, Joonpyo, Arndt, Claudia, Bannink, André, Bayat, Ali R., Brito, André F., Boland, Tommy, Casper, David, Crompton, Les A., Dijkstra, Jan, Eugène, Maguy A., Garnsworthy, Phil C., Haque, Md Najmul, Hellwing, Anne L. F., Huhtanen, Pekka, Kreuzer, Michael, Kuhla, Bjoern, Lund, Peter, Madsen, Jørgen, Martin, Cécile, McClelland, Shelby C., McGee, Mark, Moate, Peter J., Muetzel, Stefan, Muñoz, Camila, O'Kiely, Padraig, Peiren, Nico, Reynolds, Christopher K., Schwarm, Angela, Shingfield, Kevin J., Storlien, Tonje M., Weisbjerg, Martin R., Yáñez‐Ruiz, David R., Yu, Zhongtang

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